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Daily longitudinal sampling of SARS-CoV-2 infection reveals substantial heterogeneity in infectiousness.

Ruian KePamela P MartinezRebecca Lee SmithLaura L GibsonAgha MirzaMadison ConteNicholas GallagherChun Huai LuoJunko JarrettRuifeng ZhouAbigail R ConteTongyu LiuMireille FarjoKimberly K O WaldenGloria RendonChristopher J FieldsLeyi WangRichard FredricksonDarci C EdmonsonMelinda E BaughmanKaren K ChiuHannah ChoiKevin R ScardinaShannon BradleyStacy L GlossCrystal A ReinhartJagadeesh YedetoreJessica QuicksallAlyssa N OwensJohn BroachBruce BartonPeter LazarWilliam J HeetderksMatthew L RobinsonHeba H MostafaYukari C ManabeAndrew S PekoszDavid D McManusChristopher B Brooke
Published in: Nature microbiology (2022)
The dynamics of SARS-CoV-2 replication and shedding in humans remain poorly understood. We captured the dynamics of infectious virus and viral RNA shedding during acute infection through daily longitudinal sampling of 60 individuals for up to 14 days. By fitting mechanistic models, we directly estimated viral expansion and clearance rates and overall infectiousness for each individual. Significant person-to-person variation in infectious virus shedding suggests that individual-level heterogeneity in viral dynamics contributes to 'superspreading'. Viral genome loads often peaked days earlier in saliva than in nasal swabs, indicating strong tissue compartmentalization and suggesting that saliva may serve as a superior sampling site for early detection of infection. Viral loads and clearance kinetics of Alpha (B.1.1.7) and previously circulating non-variant-of-concern viruses were mostly indistinguishable, indicating that the enhanced transmissibility of this variant cannot be explained simply by higher viral loads or delayed clearance. These results provide a high-resolution portrait of SARS-CoV-2 infection dynamics and implicate individual-level heterogeneity in infectiousness in superspreading.
Keyphrases
  • sars cov
  • respiratory syndrome coronavirus
  • high resolution
  • single cell
  • gene expression
  • cross sectional
  • liver failure
  • hepatitis b virus
  • mass spectrometry
  • genome wide
  • high speed